Clinical trial · Interventional
Safety and Biomarker of OPB-111077 in Subjects With Advanced Solid Tumor
A Phase 1, Open-label, Non-Randomized, Dose Escalation Trial to Evaluate Safety and Biomarker of OPB-111077 in Subjects With Advanced Solid Tumor
NCT02250170CI-TRIAL-00040505completedPhase 1ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This open-label, non-randomized trial will comprise of 2 parts. A dose escalation part will characterize the safety, biomarker and pharmacokinetics of OPB-111077 in advanced solid tumor. Subsequently, an expansion part will further evaluate the biomarker, safety, pharmacokinetics and antitumor activity of OPB-111077 in selected tumor types.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Solid Tumor | Solid Neoplasm | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| OPB-111077 | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- OPB-111077
- description
- Tablet, Oral, 300mg/500mg/700mg/900mg 4 days-on \& 3 days-off (21 days=1cycle)
- interventionNames
- Drug: OPB-111077
Primary outcomes (3)
- measure
- Adverse Events
- timeFrame
- 21 days
- description
- Number of participants with Adverse Events
- measure
- Maximum tolerated dose
- timeFrame
- 21 days
- description
- The highest dose that does not lead to discontinuation of dose escalation
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 20 Years
- Maximum age
- 80 Years
Show eligibility criteria text
Inclusion Criteria: 1. Pathologically and/or cytologically confirmed advanced solid tumor 2. Patients who were refractory to standard therapy or for which there are no standard treatment options available 3. Age 20 to 80 years at the time of informed consent 4. Patients who, together with their partner, are willing and capable of using an appropriate method of contraception throughout the trial period and until at least 12 weeks after final IMP administration 5. Patients informed of the diagnosis of advanced solid tumor who are fully informed about the content of the study by the investigator or subinvestigator using the specified written consent form and other written explanation, and give written consent to participate in the study of their free will 6. Patients who are able to take oral medication Exclusion Criteria: 1. Patients with symptomatic brain metastases 2. Patients who have not recovered from any prior therapy related toxicity deemed to be clinically significant at study entry, except for the test item defined in inclusion criteria. 3. Patients with active infections needing whole body therapy 4. Patients with positive hepatitis B surface (HBs) antigen or positive hepatitis C virus (HCV) antibody 5. Patients with positive human immunodeficiency virus (HIV) antibody 6. Patients with uncontrollable cardiac diseases 7. Patients with uncontrollable pain by analgesic drugs 8. Patients with a history of organ transplantation 9. Patients who have received another IMP 10. Patients who are pregnant, possibly pregnant, or lactating 11. Patients otherwise judged by the investigator or subinvestigator to be inappropriate for inclusion in the trial
References
Publications (0)
Data not yet available
No reference posted for this study.